Canonical Allele Identifier: CA1600011
Gene: SRD5A2 HGNC NCBI

Linked Data

dbSNP Id: rs371573955
gnomAD v2: 2-31805772-T-A
gnomAD v3: 2-31580702-T-A
gnomAD v4: 2-31580702-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.31580702T>A , CM000664.2:g.31580702T>A GRCh38
NC_000002.11:g.31805772T>A , CM000664.1:g.31805772T>A GRCh37
NC_000002.10:g.31659276T>A NCBI36
NG_008365.1:g.5270A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000622030.2:c.199A>T MANE Select ENSP00000477587.1:p.Ile67Phe
ENST00000622030.1:c.199A>T ENSP00000477587.1:p.Ile67Phe
NM_000348.3:c.199A>T NP_000339.2:p.Ile67Phe
XM_011533068.1:c.199A>T XP_011531370.1:p.Ile67Phe
XM_011533070.1:c.27-46936A>T XP_011531372.1:n.27-46936A>T
XM_011533071.1:c.27-46936A>T XP_011531373.1:n.27-46936A>T
XM_011533072.1:c.27-46936A>T XP_011531374.1:n.27-46936A>T
XM_011533072.2:c.27-46936A>T XP_011531374.1:n.27-46936A>T
NM_000348.4:c.199A>T MANE Select NP_000339.2:p.Ile67Phe